Variant report

Variant	rs7723549
Chromosome Location	chr5:57766682-57766683
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10076546	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10471452	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11948619	1.00[ASN][1000 genomes]
rs11950875	1.00[ASN][1000 genomes]
rs1508918	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1508919	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs154489	0.91[ASN][1000 genomes]
rs154676	0.91[ASN][1000 genomes]
rs154677	0.91[ASN][1000 genomes]
rs2216691	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2591860	0.91[ASN][1000 genomes]
rs2662619	0.85[AMR][1000 genomes]
rs32617	0.94[ASN][1000 genomes]
rs4699927	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4700287	0.85[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4700290	0.89[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs4700293	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs55906147	0.97[ASN][1000 genomes]
rs62366398	0.82[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs695921	0.91[ASN][1000 genomes]
rs7726165	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7729581	0.82[AMR][1000 genomes]
rs7729588	0.83[AMR][1000 genomes]
rs7730200	0.91[AMR][1000 genomes]
rs861293	0.90[ASN][1000 genomes]
rs863846	0.91[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57763000-57771000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:57766200-57766800	Enhancers	Monocytes-CD14+_RO01746	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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